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Pressure injuRy preventiOn by inTermittent EleCtrical sTimulation

NCT04328246 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 4

Last updated 2023-01-11

No results posted yet for this study

Summary

The proposed study assesses the superiority of IES supplementation to the standard of care alone (offloading pressure every two hours) in improving the prevention and treatment of sacral and ischial pressure injuries.

Conditions

  • Pressure Injury

Interventions

DEVICE

IES System

The IES system is composed of a stimulator and self-adhesive surface gel electrodes.

OTHER

Standard of Care Therapy

Standard institutional practices for treating pressure injury.

Sponsors & Collaborators

  • Rehabtronics

    collaborator UNKNOWN

  • AHS Cancer Control Alberta

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-02-26
Primary Completion
2022-03-14
Completion
2022-03-14

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04328246 on ClinicalTrials.gov